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Sensitivity of the Social Behavior Observer Checklist to Early Symptoms of Patients With Frontotemporal Dementia.
Toller G, Cobigo Y, Ljubenkov PA, Appleby BS, Dickerson BC, Domoto-Reilly K, Fong JC, Forsberg LK, Gavrilova RH, Ghoshal N, Heuer HW, Knopman DS, Kornak J, Lapid MI, Litvan I, Lucente DE, Mackenzie IR, McGinnis SM, Miller BL, Pedraza O, Rojas JC, Staffaroni AM, Wong B, Wszolek ZK, Boeve BF, Boxer AL, Rosen HJ, Rankin KP; and the ALLFTD research consortium. Toller G, et al. Among authors: wszolek zk. Neurology. 2022 Aug 1;99(5):e488-e499. doi: 10.1212/WNL.0000000000200582. Neurology. 2022. PMID: 35584922 Free PMC article.
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).
Tsuboi Y, Baker M, Hutton ML, Uitti RJ, Rascol O, Delisle MB, Soulages X, Murrell JR, Ghetti B, Yasuda M, Komure O, Kuno S, Arima K, Sunohara N, Kobayashi T, Mizuno Y, Wszolek ZK. Tsuboi Y, et al. Among authors: wszolek zk. Neurology. 2002 Dec 10;59(11):1791-3. doi: 10.1212/01.wnl.0000038909.49164.4b. Neurology. 2002. PMID: 12473774
Parkinson disease: handedness predicts asymmetry.
Uitti RJ, Baba Y, Whaley NR, Wszolek ZK, Putzke JD. Uitti RJ, et al. Among authors: wszolek zk. Neurology. 2005 Jun 14;64(11):1925-30. doi: 10.1212/01.WNL.0000163993.82388.C8. Neurology. 2005. PMID: 15955945
Gender and the Parkinson's disease phenotype.
Baba Y, Putzke JD, Whaley NR, Wszolek ZK, Uitti RJ. Baba Y, et al. Among authors: wszolek zk. J Neurol. 2005 Oct;252(10):1201-5. doi: 10.1007/s00415-005-0835-7. Epub 2005 Sep 12. J Neurol. 2005. PMID: 16151602
Lrrk2 and Lewy body disease.
Ross OA, Toft M, Whittle AJ, Johnson JL, Papapetropoulos S, Mash DC, Litvan I, Gordon MF, Wszolek ZK, Farrer MJ, Dickson DW. Ross OA, et al. Among authors: wszolek zk. Ann Neurol. 2006 Feb;59(2):388-93. doi: 10.1002/ana.20731. Ann Neurol. 2006. PMID: 16437559
Pathophysiology of REM sleep behaviour disorder and relevance to neurodegenerative disease.
Boeve BF, Silber MH, Saper CB, Ferman TJ, Dickson DW, Parisi JE, Benarroch EE, Ahlskog JE, Smith GE, Caselli RC, Tippman-Peikert M, Olson EJ, Lin SC, Young T, Wszolek Z, Schenck CH, Mahowald MW, Castillo PR, Del Tredici K, Braak H. Boeve BF, et al. Brain. 2007 Nov;130(Pt 11):2770-88. doi: 10.1093/brain/awm056. Epub 2007 Apr 5. Brain. 2007. PMID: 17412731 Review.
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Rademakers R, Baker M, Gass J, Adamson J, Huey ED, Momeni P, Spina S, Coppola G, Karydas AM, Stewart H, Johnson N, Hsiung GY, Kelley B, Kuntz K, Steinbart E, Wood EM, Yu CE, Josephs K, Sorenson E, Womack KB, Weintraub S, Pickering-Brown SM, Schofield PR, Brooks WS, Van Deerlin VM, Snowden J, Clark CM, Kertesz A, Boylan K, Ghetti B, Neary D, Schellenberg GD, Beach TG, Mesulam M, Mann D, Grafman J, Mackenzie IR, Feldman H, Bird T, Petersen R, Knopman D, Boeve B, Geschwind DH, Miller B, Wszolek Z, Lippa C, Bigio EH, Dickson D, Graff-Radford N, Hutton M. Rademakers R, et al. Lancet Neurol. 2007 Oct;6(10):857-68. doi: 10.1016/S1474-4422(07)70221-1. Lancet Neurol. 2007. PMID: 17826340
699 results